Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/- | Ancestral: C | MAF: 0.45 (-)
Location

Chromosome 11:102799765 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

This variation has 4 HGVS names - click the plus to show

11:g.102799765delC
ENST00000525739.5:n.682+1643delC
ENST00000371455.6:n.423+1643delC
ENST00000544704.1:n.443+1643delC

About this variant

This variant overlaps 5 transcripts, has 1175 individual genotypes, is associated with 4 phenotypes and is mentioned in 55 citations.

Variation displays